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22. New Zealand Bioethics Conference February 2004: emerging biotechnologies: ethics and regulation. Evans D N Z Bioeth J; 2004 Feb; 5(1):16-21. PubMed ID: 15597488 [No Abstract] [Full Text] [Related]
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27. Proposed model ethical protocol for collecting DNA samples. Weiss KM; Cavalli-Sforza LL; Dunston GM; Feldman M; Greely HT; Kidd KK; King M; Moore JA; Szathmary E; Twinn CM; Houst Law Rev; 1997; 33(5):1431-74. PubMed ID: 12627556 [No Abstract] [Full Text] [Related]
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32. The Human Genome Diversity Project and its implications for indigenous peoples. Harry D Genewatch; 1996 Oct; 10(2-3):8-9. PubMed ID: 11660352 [No Abstract] [Full Text] [Related]
33. United States regulatory requirements for research involving human subjects. J Biolaw Bus; 1998; 1(2):39-53. PubMed ID: 12739542 [No Abstract] [Full Text] [Related]
34. Building a new culture of ethics in research involving humans in Brazil. Pessini L Not Polit; 2002; 18(67):101-12. PubMed ID: 15282926 [No Abstract] [Full Text] [Related]
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36. In harm's way: research subjects who are decisionally impaired. Sundram CJ J Health Care Law Policy; 1998; 1(1):36-65. PubMed ID: 15573429 [No Abstract] [Full Text] [Related]
38. Children as research subjects: a proposal to revise the current federal regulations using a moral framework. Ross LF Stanford Law Pol Rev; 1997; 8(1):159-76. PubMed ID: 16528858 [No Abstract] [Full Text] [Related]
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